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1 evirus A21, an EV with tropism for the human intercellular adhesion molecule 1 (hICAM-1), through ser
2 human melanoma cell line (Lu1205) increased intercellular adhesion molecule 1 (ICAM-1) and E-selecti
4 the proinflammatory cell adhesion molecules intercellular adhesion molecule 1 (ICAM-1) and vascular
5 e endothelium and in adhesion to immobilized intercellular adhesion molecule 1 (ICAM-1) and vascular
6 ed protein kinases (MAPKs) and expression of intercellular adhesion molecule 1 (ICAM-1) and vascular
7 ction associated antigen 1 (LFA-1) binds the intercellular adhesion molecule 1 (ICAM-1) by its alpha(
8 In this study, the binding affinity of human intercellular adhesion molecule 1 (ICAM-1) chimera and l
9 ezrin/radixin/moesin (ERM) phosphorylation, intercellular adhesion molecule 1 (ICAM-1) clustering, a
10 Infected IL-17R-deficient corneas had low intercellular adhesion molecule 1 (ICAM-1) expression, a
13 to LLV was able to trigger the clustering of intercellular adhesion molecule 1 (ICAM-1) on endothelia
14 ascular cell adhesion molecule (VCAM-1), and intercellular adhesion molecule 1 (ICAM-1) on endothelia
15 scribed as an inflammatory disease, in which intercellular adhesion molecule 1 (ICAM-1) plays a key r
16 re we show that HDL suppresses expression of intercellular adhesion molecule 1 (ICAM-1) through the t
17 shown to bind to several receptors, of which intercellular adhesion molecule 1 (ICAM-1) upregulation
20 the NF-kappaB pathway instantly upregulates intercellular adhesion molecule 1 (ICAM-1) which binds i
22 ction also increased the cellular content of intercellular adhesion molecule 1 (ICAM-1), a molecule i
23 ow a group of PfEMP1 proteins interacts with intercellular adhesion molecule 1 (ICAM-1), allowing us
25 rogenic TGRL increased expression of VCAM-1, intercellular adhesion molecule 1 (ICAM-1), and E-select
26 Leukocyte infiltration, improved levels of intercellular adhesion molecule 1 (ICAM-1), and oxidativ
27 tenuated the over expression of VEGF and the intercellular adhesion molecule 1 (ICAM-1), and reduced
28 gnificant in only 1 replication set included intercellular adhesion molecule 1 (ICAM-1), anti-LG3, am
29 "outside-in" signaling when bound to ligand intercellular adhesion molecule 1 (ICAM-1), but little i
30 vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule 1 (ICAM-1), E-selectin,
31 d inflammation: coagulation factor III (F3), intercellular adhesion molecule 1 (ICAM-1), interferon g
32 tu-like expression of cadherins, E-selectin, intercellular adhesion molecule 1 (ICAM-1), vascular cel
33 ance of a cellular adhesion protein known as intercellular adhesion molecule 1 (ICAM-1), which helps
34 We examined human effector T lymphocytes on intercellular adhesion molecule 1 (ICAM-1)-coated surfac
35 l host factors impacting protection included intercellular adhesion molecule 1 (ICAM-1)-dependent pol
36 cell morphology alterations, and crawling on intercellular adhesion molecule 1 (ICAM-1)-expressing ce
39 nt/beta-catenin signaling in AECs attenuated intercellular adhesion molecule 1 (ICAM-1)/vascular cell
40 d proteins HLA-A, HLA-B, and HLA-C antigens; intercellular adhesion molecule 1 (ICAM-1); S100; transc
41 in T cells increased expression of IFNG and intercellular adhesion molecule 1 (ICAM1) and induced T-
42 , unlike amphiregulin and TNFRI, full-length intercellular adhesion molecule 1 (ICAM1) is released fr
43 pression of asparaginyl endopeptidase (AEP), intercellular adhesion molecule 1 (ICAM1), and ras-relat
44 monocyte chemoattractant protein-1 (MCP-1), intercellular adhesion molecule 1 (ICAM1), F4/80, plasmi
45 out mice originated from decreased levels of intercellular adhesion molecule 1 (ICAM1)/vascular cell
47 t of BMI on inflammatory biomarkers [soluble intercellular adhesion molecule 1 (sICAM-1), high sensit
48 otein (hs-CRP), adiponectin, leptin, soluble intercellular adhesion molecule 1 (sICAM-1), soluble vas
49 han antibodies to transferrin receptor-1 and intercellular adhesion molecule 1 (TfR-1 and ICAM-1).
50 IL-6], IL-8, IL-1alpha, CXCL1, CXCL2, CXCL3, intercellular adhesion molecule 1 [ICAM1]), chemoattract
51 s and to enhanced cell-surface expression of intercellular adhesion molecule 1 and altered expression
52 stained positive for 2 inflammatory markers, intercellular adhesion molecule 1 and interleukin 8.
54 L oxidation and 2) a significant decrease in intercellular adhesion molecule 1 and OLR1 gene expressi
56 munoblots were used to measure expression of intercellular adhesion molecule 1 and the inducible form
57 n the luminal surface, such as clustering of intercellular adhesion molecule 1 and vascular cell adhe
58 egulation of the cellular adhesion molecules Intercellular Adhesion Molecule 1 and Vascular Cell Adhe
59 dies against Macrophage-1 antigen (Mac-1) or intercellular adhesion molecule 1 and were reproduced in
60 ion of NF-kappaB, which in turn up-regulated intercellular adhesion molecule 1 as evident from chroma
61 D showed increased endothelial inflammation (intercellular adhesion molecule 1 expression) and increa
62 -1 displayed an attenuated interleukin-6 and intercellular adhesion molecule 1 expression, resulting
65 the lymphocyte function-associated antigen 1-intercellular adhesion molecule 1 interaction, reduced T
68 cantly increased KC numbers via induction of intercellular adhesion molecule 1 on liver sinusoidal en
69 trast to most other rhinoviruses, which bind intercellular adhesion molecule 1 receptors via a capsid
70 the expression of endothelial E-selectin and intercellular adhesion molecule 1 was decreased by eithe
73 ession for ACE2 and TMPRSS2, and for ICAM-1 (intercellular adhesion molecule 1) (rhinovirus receptor
74 e function-associated antigen 1) for ICAM-1 (intercellular adhesion molecule 1) but significantly low
75 n 6, tumor necrosis factor alpha and soluble intercellular adhesion molecule 1) were unsuitable for p
78 phaIIbbeta3 with endothelial alphavbeta3 and intercellular adhesion molecule 1, and (3) a stimulatory
79 4 BCC tumor mRNA markers (CD25, CD3epsilon, intercellular adhesion molecule 1, and CD68) that have b
80 lpha, interleukin (IL)-1beta, IL-6, KC/IL-8, intercellular adhesion molecule 1, and cluster of differ
81 active protein, adiponectin, leptin, soluble intercellular adhesion molecule 1, and E-selectin all fe
82 s showed increased interleukin (IL)-6, IL-8, intercellular adhesion molecule 1, and platelet endothel
83 elated adhesion molecules (e.g., P-selectin, intercellular adhesion molecule 1, and vascular cell adh
84 chemistry of eNOS, endothelin-1, P-selectin, intercellular adhesion molecule 1, and vascular cell adh
85 or necrosis factor alpha, caspase-1 (CASP1), intercellular adhesion molecule 1, IL-10, heme oxygenase
86 anulocyte colony-stimulating factor, soluble intercellular adhesion molecule 1, macrophage migration-
87 selectin, vascular cell adhesion molecule 1, intercellular adhesion molecule 1, platelet endothelial
88 ceptor-2, vascular cell adhesion molecule 1, intercellular adhesion molecule 1, selectins, and integr
89 ld increase in the expression of E-selectin, intercellular adhesion molecule 1, vascular cell adhesio
90 sinophils also showed enhanced expression of intercellular adhesion molecule 1, which depended on dir
91 s also associated with the overexpression of intercellular adhesion molecule 1, which is expressed on
92 ng Raman-active molecules were conjugated to intercellular adhesion molecule 1- (ICAM-1-) specific mo
93 induced pulmonary inflammation, with altered intercellular adhesion molecule 1-dependent slow neutrop
96 ntiation, respectively; the plasma levels of intercellular adhesion molecule 1; and CCR6 expression i
97 th factor beta1 and beta2; thrombospondin 2; intercellular adhesion molecule 1; interleukin 6 [IL-6];
98 rs of endothelial adhesion (sICAM-1 [soluble intercellular adhesion molecule 1] and sVCAM-1 [soluble
100 endothelial cells had higher levels of ICAM (intercellular adhesion molecule)-1 and TF expression fol
101 creased vascular inflammation marker soluble intercellular adhesion molecule-1 (-10%, P < 0.01).
102 r alpha receptor II (B = 0.07, p < .01), and intercellular adhesion molecule-1 (B = 0.04, p < .05) le
103 efined as CD146(+)CD45(-)) exhibit increased intercellular adhesion molecule-1 (CD54) and Fas in resp
104 NOS), nuclear factor-kappa B (NF-kappaB) and intercellular adhesion molecule-1 (ICAM) (P < 0.001, res
105 endothelial adhesion molecules, particularly intercellular adhesion molecule-1 (ICAM-1) and a subsequ
106 ) to circulating pro-inflammatory cytokines, intercellular adhesion molecule-1 (ICAM-1) and acute cor
107 f these cells, concomitant with reduction of intercellular adhesion molecule-1 (ICAM-1) and diminishi
108 contact points for the known HRV receptors, intercellular adhesion molecule-1 (ICAM-1) and low-densi
109 t3 interaction in correlation with increased intercellular adhesion molecule-1 (ICAM-1) and soluble-I
110 lls, we found that GPx-1 deficiency augments intercellular adhesion molecule-1 (ICAM-1) and vascular
111 ular endothelium on which ligands, including intercellular adhesion molecule-1 (ICAM-1) and vascular
112 otential of these cells through reduction of intercellular adhesion molecule-1 (ICAM-1) and vascular
113 udy was to identify mechanisms through which intercellular adhesion molecule-1 (ICAM-1) augments the
116 tumor necrosis factor-alpha (TNF-alpha) and intercellular adhesion molecule-1 (ICAM-1) in aqueous hu
117 Herein, we describe the overexpression of intercellular adhesion molecule-1 (ICAM-1) in human TNBC
118 ntigen-1 (LFA-1) interaction with its ligand intercellular adhesion molecule-1 (ICAM-1) induces a gen
121 sion and display high spontaneous binding to intercellular adhesion molecule-1 (ICAM-1) ligand under
123 recognition of pMHC and the adhesion ligand intercellular adhesion molecule-1 (ICAM-1) on supported
124 called 3DNA coupled with antibodies against intercellular adhesion molecule-1 (ICAM-1), a glycoprote
126 NAME also blocked blast-induced increases in intercellular adhesion molecule-1 (ICAM-1), a molecule t
127 using polymer nanocarriers (NCs) targeted to intercellular adhesion molecule-1 (ICAM-1), an endotheli
128 PfEMP1 and human endothelial proteins CD36, intercellular adhesion molecule-1 (ICAM-1), and endothel
129 tor inhibitor-1, soluble E-selectin, soluble intercellular adhesion molecule-1 (ICAM-1), and soluble
130 scular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1), endothelial
131 elial migration mediated by a combination of intercellular adhesion molecule-1 (ICAM-1), vascular adh
132 t endothelial adhesion molecule-1 (PECAM-1), intercellular adhesion molecule-1 (ICAM-1), vascular adh
133 pha by restraining the induced expression of intercellular adhesion molecule-1 (ICAM-1), vascular cel
134 sation requires selectin-mediated tethering, intercellular adhesion molecule-1 (ICAM-1)-dependent fir
135 ated neutrophils, microglia/macrophages, and intercellular adhesion molecule-1 (ICAM-1)-positive bloo
144 urface proteins, including CD69, L-selectin, intercellular adhesion molecule-1 (ICAM-1, CD54), CD44,
145 ster of differentiation 8a (Cd8a), Cd14, and intercellular adhesion molecule-1 (Icam1) by about two-f
146 in mice, these progenitor cells give rise to intercellular adhesion molecule-1 (ICAM1)/CD54-expressin
147 ine to 2-month follow-up in concentration of intercellular adhesion molecule-1 (P < .001), interleuki
148 the prospective association between soluble intercellular adhesion molecule-1 (sICAM-1) and cancer r
149 dence of proliferative DR (PDR), and soluble intercellular adhesion molecule-1 (sICAM-1) and TNF-alph
150 active protein (CRP), serum amyloid A (SAA), intercellular adhesion molecule-1 (sICAM-1) and vascular
151 e measured levels of UA and soluble forms of intercellular adhesion molecule-1 (sICAM-1), vascular ce
154 crosis Factor receptor II [sTNFRII], soluble Intercellular Adhesion Molecule-1 [sICAM-1]), angiogenic
156 [sRAGE]) and endothelial biomarkers (soluble intercellular adhesion molecule-1 and endocan [full-leng
157 n, including the metastasis-related proteins intercellular adhesion molecule-1 and urokinase-type pla
160 A1 exon skipping mutations had higher plasma intercellular adhesion molecule-1 and vascular cell adhe
161 , CCL5, and CCL20 and the adhesion molecules intercellular adhesion molecule-1 and vascular cell adhe
162 re, CB2R agonists decreased the induction of intercellular adhesion molecule-1 and vascular cell adhe
163 alpha receptor II) and endothelial function (intercellular adhesion molecule-1 and vascular cell adhe
164 ference studies identified interleukin-6 and intercellular adhesion molecule-1 as key NF-kappaB targe
167 ced tumor necrosis factor (TNF)alpha-induced intercellular adhesion molecule-1 expression and attenua
168 eling-positive cells, TNF-alpha release, and intercellular adhesion molecule-1 expression compared wi
169 ase products and IL-10 and reduced CD11b and intercellular adhesion molecule-1 expression on neutroph
170 leased platelet miR-320b on endothelial cell intercellular adhesion molecule-1 expression was shown.
171 reased vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression, and neutro
172 Removal of P-Rex1 significantly reduced intercellular adhesion molecule-1 expression, polymorpho
173 anism and induced an increase in endothelial intercellular adhesion molecule-1 expression, production
174 helial vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression, reduced in
176 treatment failed to inhibit TNFalpha-induced intercellular adhesion molecule-1 expression, treatment
180 ges have been assumed to mediate adhesion to intercellular adhesion molecule-1 for T-cell conjugation
181 ses in vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 mRNA expression in the
183 es produced greater levels of chemokines and intercellular adhesion molecule-1 that are associated wi
185 spleen tyrosine kinase and cell adhesion to intercellular adhesion molecule-1 under dynamic flow.
186 n-8, monocyte chemoattactrant protein-1, and intercellular adhesion molecule-1 were analyzed after tr
187 e vascular cell adhesion molecule-1, soluble intercellular adhesion molecule-1) and immune (soluble t
188 uced pulmonary adhesion molecule expression (intercellular adhesion molecule-1) and tissue infiltrati
190 activator [tPA]) and endothelial activation (intercellular adhesion molecule-1) in serial biopsies ob
192 ons of vascular cell adhesion molecule-1 and intercellular adhesion molecule-1, albeit less efficient
193 ssion of vascular endothelial growth factor, intercellular adhesion molecule-1, and tumor necrosis fa
194 unds of RW decreased serum concentrations of intercellular adhesion molecule-1, E-selectin, and IL-6
195 expression of NF-kappaB target genes VCAM-1, intercellular adhesion molecule-1, E-selectin, and tissu
196 rial loads were associated with higher serum intercellular adhesion molecule-1, E-selectin, and vascu
197 selectin, vascular cell adhesion molecule-1, intercellular adhesion molecule-1, fibrinogen-like prote
199 nd inflammatory markers [C-reactive protein, intercellular adhesion molecule-1, interleukin-6, and tu
200 high-sensitivity C-reactive protein, soluble intercellular adhesion molecule-1, leptin, hemoglobin A(
201 Model 3 identified a set of 6 biomarkers (intercellular adhesion molecule-1, matrix metalloprotein
202 iomarkers strongly associated with death/MI: intercellular adhesion molecule-1, matrix metalloprotein
203 osis protein-2, cyclin D1, cyclooxygenase-2, intercellular adhesion molecule-1, matrix metalloprotein
204 enofibrate also attenuated overexpression of intercellular adhesion molecule-1, monocyte chemoattract
205 ession of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, monocyte chemoattract
206 ut reduced expression or secretion of T-bet, intercellular adhesion molecule-1, nucleotide-binding ol
207 th changes in von Willebrand factor, soluble intercellular adhesion molecule-1, soluble E-Selectin, P
208 levels of C-reactive protein, interleukin-6, intercellular adhesion molecule-1, soluble tumor necrosi
209 , angiopoietin-1 and angiopoietin-2, soluble intercellular adhesion molecule-1, soluble vascular cell
210 sitivity C-reactive protein, fibrinogen, and intercellular adhesion molecule-1, suggested that GlycA
211 or necrosis factor-alpha, interleukin-6, and intercellular adhesion molecule-1, than iron-overloaded
213 e chemotactic protein-1, C-reactive protein, intercellular adhesion molecule-1, vascular cell adhesio
214 (tumor necrosis factor-alpha, interleukin-6, intercellular adhesion molecule-1, vascular cell adhesio
215 gamma), endothelial cell adhesion molecules (intercellular adhesion molecule-1, vascular cell adhesio
216 ay and expression of cell adhesion molecules intercellular adhesion molecule-1, vascular cell adhesio
217 ecreted levels of the proangiogenic proteins intercellular adhesion molecule-1, vascular cell adhesio
218 microscopy and contrast-enhanced ultrasound, intercellular adhesion molecule-1-targeted and rhodamine
220 s were translatable in vivo, confirming that intercellular adhesion molecule-1-targeted and rhodamine
227 ls of plasma endothelial biomarkers (soluble intercellular adhesion molecule-1: OR, 1.58; 95% CI, 1.2
228 M [vascular cell adhesion molecule-1], ICAM [intercellular adhesion molecule-1], and MCP1 [monocyte c
229 huTreg, or their respective porcine ligands intercellular adhesion molecule 2 (CD102) and vascular c
230 sured on choroidal-scleral flat mounts using intercellular adhesion molecule 2 immunofluorescence sta
232 ard this goal, we recently demonstrated that intercellular adhesion molecule-2 (ICAM-2) converted neu
233 and beta1, and their counterligands, such as intercellular adhesion molecule-2 and P-selectin, in bre
234 on Willebrand factor [vWF], VE-cadherin, and intercellular adhesion molecule-2), but not all (eg, VEG
236 eting the C-type lectin receptor DC-specific intercellular adhesion molecule 3-grabbing nonintegrin (
237 and 2, dectin 1, and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin i
238 annose receptor- and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin-m
239 engulfed by mucosal dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin-p
240 better interaction with DC-SIGN [DC-specific intercellular adhesion molecule-3 (ICAM-3)-grabbing noni
241 the C-type lectins, dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin
242 r binding toward the dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin
243 ans cells (LCs), and dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin
244 or downregulation of dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin
245 face lectin DC-SIGN (dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin)
247 R, efficiently bound dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
248 the C-type lectin receptor (CLR) DC-specific intercellular adhesion molecule-3-grabbing nonintegrin (
249 recognition receptor dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
250 was not mediated by dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
251 r receptors, such as dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
252 s able to bind human dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
253 receptors, including dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
254 pressing the lectins dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
255 the lectin receptor dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (
258 ding molecules CCR5, dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin,
259 CD3, CCR5, Langerin, dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin,
260 d F(ab')2 fragments of IVIg with DC-specific intercellular adhesion molecule-3-grabbing nonintegrin.
261 repeats and discoidin I-like domains 3, and intercellular adhesion molecule 4; the first three have
262 ecule (BCAM/Lu) and ECM laminin, and between intercellular adhesion molecule-4 (ICAM-4) and endotheli
263 RBCs to endothelial cells is mediated by the intercellular adhesion molecule-4 (ICAM-4), which appear
268 f) ligand 2, neuron-specific enolase, S100b, intercellular adhesion molecule-5, and brain-derived neu
270 -1, Bax and caspase-3, protein expression of intercellular adhesion molecule as well as the number of
271 Soluble endothelial selectin and soluble intercellular adhesion molecule concentrations decreased
272 that AP-1 regulates the localization of the intercellular adhesion molecule E-cadherin and that loss
273 duced pulmonary interleukin-6 transcription, intercellular adhesion molecule expression, neutrophil i
275 NFAT-independent adhesion of T cells to the intercellular adhesion molecule ICAM-1, with little effe
276 t but is essential for efficient adhesion to intercellular adhesion molecule (ICAM) 1 and vascular ce
277 retained locally through constitutive LFA-1-intercellular adhesion molecule (ICAM) 1 interactions.
278 cular cell adhesion molecule (VCAM), but not intercellular adhesion molecule (ICAM), suggesting they
280 exhibiting a 70 and 50% increase in retinal intercellular adhesion molecule (ICAM)-1 expression and
282 ctivity of platelets taken from mice lacking intercellular adhesion molecule (ICAM)-1 identified a ma
283 nied by significant reduction of circulating intercellular adhesion molecule (ICAM)-1 was observed.
284 ng loops in vascular cell adhesion molecule, intercellular adhesion molecule (ICAM)-1, ICAM-2, ICAM-3
285 In the validation cohort concentrations of intercellular adhesion molecule (ICAM)-1, IL-8, and vasc
290 al region includes selected residues from an intercellular adhesion molecule (ICAM)-like motif shared
292 igen-1 (LFA-1; integrin alpha(L)beta(2)) for intercellular adhesion molecules (ICAMs) on endothelia o
293 rations in the jugular bulb, whereas soluble intercellular adhesion molecule increased significantly
294 ve activities involved CD40, CD80, CD86, and intercellular adhesion molecule interactions and require
295 ndent decrease in cell surface levels of the intercellular adhesion molecule PECAM-1 (CD31) when exam
297 spine apparatus, and telencephalin (TLCN, or intercellular adhesion molecule type 5), a protein assoc
298 h factor, von Willebrand factor, E-selectin, intercellular adhesion molecule, vascular cell adhesion
299 e kinase, von Willebrand factor, E-selectin, intercellular adhesion molecule, vascular cell adhesion